ZFIN ID: ZDB-LAB-070723-1
Institut de Recherche en Ophtalmologie (IRO)
PI/Director: Schorderet, Daniel
Contact Person: Schorderet, Daniel
Email: gaelle.boisset@irovision.ch
URL: http://www.irovision.ch/
Address: 64, Av. du Gd-Champsec Case Postale 4168 CH-1950 Sion 4 SWITZERLAND
Country: Switzerland
Phone: +41 (0)27 205 79 00
Fax: +41 (0)27 205 79 01
Line Designation: iro


GENOMIC FEATURES ORIGINATING FROM THIS LAB
Show all 1 genomic features


STATEMENT OF RESEARCH INTERESTS


LAB MEMBERS
Renner, Nicole Post-Doc Delbeauve, Benoît Technical Staff Favez, Tatiana Technical Staff
Pinton, Gaëtan


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
Crippa, S., Nemir, M., Ounzain, S., Ibberson, M., Berthonneche, C., Sarre, A., Boisset, G., Maison, D., Harshman, K., Xenarios, I., Diviani, D., Schorderet, D., Pedrazzini, T. (2016) Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways. Cardiovascular research. 110(1):73-84
Marcelli, F., Boisset, G., Schorderet, D.F. (2014) A Dimerized HMX1 Inhibits EPHA6/epha4b in Mouse and Zebrafish Retinas. PLoS One. 9:e100096
Page, L., Polok, B., Bustamante, M., and Schorderet, D.F. (2013) Bigh3 Is Upregulated in Regenerating Zebrafish Fin. Zebrafish. 10(1):36-42
Boisset, G., and Schorderet, D.F. (2012) Zebrafish hmx1 promotes retinogenesis. Experimental Eye Research. 105:34-42
Slavotinek, A.M., Chao, R., Vacik, T., Yahyavi, M., Vacik, T., Abouzeid, H., Bardakjian, T., Schneider, A., Shaw, G., Sherr, E.H., Lemke, G., Youssef, M., and Schorderet, D.F. (2012) VAX1 mutation associated with microphthalmia, corpus callosum agenesis and orofacial clefting-the first description of a VAX1 phenotype in humans. Human Mutation. 33(2):364-368
Abouzeid, H., Boisset, G., Favez, T., Youssef, M., Marzouk, I., Shakankiry, N., Bayoumi, N., Descombes, P., Agosti, C., Munier, F.L., and Schorderet, D.F. (2011) Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome. American journal of human genetics. 88(1):92-98
Polok, B., Escher, P., Ambresin, A., Chouery, E., Bolay, S., Meunier, I., Nan, F., Hamel, C., Munier, F.L., Thilo, B., Mégarbané, A., and Schorderet, D.F. (2009) Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta. American journal of human genetics. 84(2):259-265
Boisset, G., Polok, B.K., and Schorderet, D.F. (2008) Characterization of pip5k3 fleck corneal dystrophy-linked gene in zebrafish. Gene expression patterns : GEP. 8(6):404-410
Schorderet, D.F., Nichini, O., Boisset, G., Polok, B., Tiab, L., Mayeur, H., Raji, B., de la Houssaye, G., Abitbol, M.M., and Munier, F.L. (2008) Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome. American journal of human genetics. 82(5):1178-1184